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131.
本文主要阐述了一种具有纤溶活性的枯草杆菌(Bacillussubtilis)蛋白激酶产生菌株的筛选与鉴定的研究结果。作者从初筛的12株Bacillussublilis菌中,通过对固体发酵和液体发酵所产生的枯草杆菌蛋白激酶,用琼脂糖-纤维蛋白平板法测其活性,经比较不同菌株的活性,筛选出两株高产酶菌株:B.subtilisHW—12和B.subtilisHW—3。同时对菌体和菌落形态特点、生理生化反应进行了鉴定,认为B.SubtilisHW-12菌株可用来做为发酵生产该酶的菌种。 相似文献
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133.
迷宫漏斗蛛Agelena labyrinthica的染色体(蜘蛛目:漏斗蛛科) 总被引:2,自引:0,他引:2
报告迷宫漏斗蛛的染色体数目、形态结构和性染色体组成。结果表明,迷宫漏斗蛛体细胞染色体数目是:雄性2n=42,雌性2n=44,性别决定机制属X_1X_2O型。X染色体是全部染色体中最长的和最短的2个(对)。染色体似乎均为端或亚端着丝粒染色体,这由C-显带标本分析所证实,没有亚中着丝粒染色体的证据。C-带标本分析表明,常染色体中,各条染色体的C-带纹,其大小和染色深浅无明显差异,但X_2染色体上有明显宽的C-带纹。C-显带处理没有得到稳定的有重复性的带纹。 相似文献
134.
朱砂叶螨羧酸脂酶最优测试条件的选择 总被引:1,自引:0,他引:1
应用二次回归通用旋转组合设计,对朱砂叶螨离体羧酸酯酶测试过程中所需缓冲液pH值、恒温时间、反应温度及底物浓度,设立4因子5水平试验,在考虑4个因子主效应和互作效应的情况下,筛选测试羧酸酯酶的最优条件组合。 相似文献
135.
建立了测定人乳腺癌胞浆cAMP结合蛋白(cAMPb.p.)方法。综合研究了其温度、保温时间、配体浓度、稳定性等条件。cAMPb.p.的K_D值为2.90×10~(-8)mol/L.并测定了60例雌激素受体(ER)Fu性乳腺癌标本的cAMPb.p.含量。此组病人术后均接受系统的内分泌治疗,ER/cAMPbp,比值范围为7.7~362×10~(-3),ER/cAMPb.p.比值≥40×10~(-3)的五年生存率明显高于比值<40×10~(-3)组,(p<0.005).表明测定ER/cAMPb.p.比值对预测患者内分泌治疗疗效,优于单独测定ER. 相似文献
136.
从人良性增生前列腺组织中经硫酸铵沉淀和肝素-琼脂糖凝胶层析纯化出人前列腺生长因子(hPGF),纯化倍数约1000倍,SDS-PAGE和等电聚焦电泳示分子量约为17kD、等电点同标准bFGF,利用分离培养的人前列腺间质成纤维细胞进行活性鉴定,发现以1.3~1.7mol/LNaCl洗脱部分为hPGF,活性最高,对间质成纤维细胞有显著刺激增殖作用。 相似文献
137.
Magnesium Adenosine 5[prime]-Triphosphate-Energized Transport of Glutathione-S-Conjugates by Plant Vacuolar Membrane Vesicles 总被引:5,自引:3,他引:2
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By characterization of the uptake of glutathione-S-conjugates, principally dinitrophenyl-S-glutathione (DNP-GS), by vacuolar membrane vesicles, we demonstrate that a subset of energy-dependent transport processes in plants are not H+-coupled but instead are directly energized by MgATP. The most salient features of this transport pathway are: (a) its specific, obligate requirement for MgATP as energy source; (b) the necessity for hydrolysis of the [gamma]-phosphate of MgATP for uptake; (c) the insensitivity of uptake to uncouplers of the transtonoplast H+ gradient (carbonylcyanide 4-trifluoromethoxyphenylhydrazone, gramicidin-D, and NH4Cl); (d) its pronounced sensitivity to vanadate and partial inhibition by vinblastine and verapamil; (e) the lack of chemical modification of DNP-GS either during or after transport; (f) the capacity of S-conjugates of chloroacetanilide herbicides, such as metolachlor-GS, but not free herbicide, to inhibit uptake; and (g) the ability of vacuolar membrane vesicles purified from a broad range of plant species, including Arabidopsis, Beta, Vigna, and Zea, to mediate MgATP-dependent, H+-electrochemical potential difference-independent DNP-GS uptake. On the basis of these findings it is proposed that the transport of DNP-GS across the vacuolar membrane of plant cells is catalyzed by a glutathione-conjugate transporter that directly employs MgATP rather than the energy contained in the transtonoplast H+-electrochemical potential difference to drive uptake. The broad distribution of the vacuolar DNP-GS transporter and its inhibition by metolachlor-GS are consistent with the notion that it plays a general role in the vacuolar sequestration of glutathione-conjugable cytotoxic agents. 相似文献
138.
A series of compounds (DAP-AA) composed of an amino acid (AA) and a dialkyl phosphoryl group (DAP) is the basic elements of life chemistry. Self-catalysis of DAP-AA gives the self-assembly oligopeptides, even in aqueous medium at 38°C. The oligo-nucleotides could also be assembled from nucleosides' phosphorylation by DAP-AA. DAP-AA acts as the energy source as well as the phosphoryl donor for the synthesis of nuclic Acids and protein. A general expression for the self assembly system is proposed. 相似文献
139.
140.
J. F. M. L. Seegers W. J. J. Meijer G. Venema S. Bron A. C. Zhao S. A. Khan 《Molecular & general genetics : MGG》1995,249(1):43-50
The single-strand origin (SSO) of the rolling-circle (RC), broad-host-range lactococcal plasmid pWVO1 was functionally characterized. The activity of this SSO in the conversion of single-stranded DNA to double-stranded DNA was tested both in vivo and in vitro. In addition, the effect of this SSO on plasmid maintenance was determined. The functional pWVO1 SSO comprises a 250 by region, containing two inverted repeats (IRs). The activity of each IR was tested, separately and in combination, in a plasmid derivative that was otherwise completely devoid of structures that might function as SSO. One of the IRs (IR 1) showed some homology with other previously described SSOs of the SSOA type, as well as with the conversion signal of the Escherichia coli phage X174. This IR was shown to have a partial, RNA polymerise-independent activity in complementary strand synthesis, both in vivo and in vitro. The second IR, which had no activity of its own, was required for full SSO activity, both in vivo and in vitro. The conversion of single-stranded DNA to the double-stranded form by the complete SSO was only partly sensitive to inhibition by rifampicin, indicating the existence of an RNA polymerase-independent pathway for this event. The results suggest that the pWVO1 SSO can be activated by two different routes: an RNA polymerise-dependent one (requiring the entire SSO), and an RNA polymerase-independent one (requiring only IR I). 相似文献